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多巴胺部分激动剂:一类新型抗精神病药物。

Dopamine partial agonists: a new class of antipsychotic.

作者信息

Lieberman Jeffrey A

机构信息

University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7160, USA.

出版信息

CNS Drugs. 2004;18(4):251-67. doi: 10.2165/00023210-200418040-00005.

Abstract

This review examines the development of dopamine partial agonists as a new class of antipsychotic agents. Partial agonists have a lower intrinsic activity at receptors than full agonists, allowing them to act either as a functional agonist or a functional antagonist, depending on the surrounding levels of naturally occurring neurotransmitter (full agonist). In the absence of a full agonist, partial agonists show functional agonist activity, binding to the receptor to produce a response. In the presence of a full agonist, partial agonists show functional antagonist activity, as receptor binding reduces the response from that seen with the full agonist. A partial agonist at dopamine D(2) receptors therefore offers an attractive option for the treatment of schizophrenia. It should act as a functional antagonist in the mesolimbic dopamine pathway, where excessive dopamine activity is thought to cause positive symptoms, but show functional agonist activity in the mesocortical pathway, where reduced dopamine activity is thought to be associated with negative symptoms and cognitive impairment. In addition, it should avoid the complete blockade of the nigrostriatal or tuberoinfundibular pathways, associated with extrapyramidal symptoms (EPS) and elevated prolactin levels, respectively. Clinical trials with aripiprazole - a new antipsychotic, which shows partial agonist activity at D(2) receptors and serotonin 5-HT(1A) receptors, and antagonist activity 5-HT(2A) receptors - have demonstrated the value of this treatment approach. Aripiprazole produced significant improvements in positive and negative symptoms in short- and long-term studies of patients with schizophrenia or schizoaffective disorder. Improvements occurred rapidly after the start of treatment, and were sustained throughout studies lasting up to 52 weeks. Significantly more patients responded to aripiprazole treatment than to haloperidol in the 52-week study, and aripiprazole-treated patients showed significantly greater improvements in negative and depressive symptoms than those receiving haloperidol. Aripiprazole treatment was well tolerated in both short- and long-term studies, showing a low liability for EPS and hyperprolactinemia, a lack of QTc prolongation, and minimal weight gain or sedation. In conclusion, the findings from clinical studies of aripiprazole show that dopamine partial agonists offer a novel, effective and well-tolerated treatment approach for patients with schizophrenia.

摘要

本综述探讨了多巴胺部分激动剂作为一类新型抗精神病药物的发展情况。部分激动剂在受体处的内在活性低于完全激动剂,这使得它们根据周围天然存在的神经递质(完全激动剂)水平,既可以作为功能性激动剂,也可以作为功能性拮抗剂发挥作用。在没有完全激动剂的情况下,部分激动剂表现出功能性激动剂活性,与受体结合以产生反应。在存在完全激动剂的情况下,部分激动剂表现出功能性拮抗剂活性,因为受体结合会降低完全激动剂所产生的反应。因此,多巴胺D(2)受体的部分激动剂为精神分裂症的治疗提供了一个有吸引力的选择。它在中脑边缘多巴胺通路中应作为功能性拮抗剂发挥作用,在该通路中多巴胺活性过高被认为会导致阳性症状,但在中脑皮质通路中表现出功能性激动剂活性,在该通路中多巴胺活性降低被认为与阴性症状和认知障碍有关。此外,它应避免完全阻断黑质纹状体或结节漏斗通路,分别与锥体外系症状(EPS)和催乳素水平升高有关。阿立哌唑——一种新型抗精神病药物,在D(2)受体和5-羟色胺5-HT(1A)受体处表现出部分激动剂活性,在5-HT(2A)受体处表现出拮抗剂活性——的临床试验证明了这种治疗方法的价值。在对精神分裂症或分裂情感性障碍患者的短期和长期研究中,阿立哌唑在阳性和阴性症状方面都产生了显著改善。治疗开始后改善迅速,并在长达52周的研究中持续存在。在52周的研究中,对阿立哌唑治疗有反应的患者明显多于接受氟哌啶醇治疗的患者,且接受阿立哌唑治疗的患者在阴性和抑郁症状方面的改善明显大于接受氟哌啶醇治疗的患者。在短期和长期研究中,阿立哌唑治疗的耐受性都很好,表现出较低的EPS和高催乳素血症风险,没有QTc延长,体重增加或镇静作用最小。总之,阿立哌唑临床研究的结果表明,多巴胺部分激动剂为精神分裂症患者提供了一种新颖、有效且耐受性良好的治疗方法。

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